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首页> 外文期刊>Nuclear Receptor Research >Therapeutic Potential of Peroxisome Proliferator-Activated Receptor Modulation in Non-Alcoholic Fatty Liver Disease and Non-Alcoholic Steatohepatitis
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Therapeutic Potential of Peroxisome Proliferator-Activated Receptor Modulation in Non-Alcoholic Fatty Liver Disease and Non-Alcoholic Steatohepatitis

机译:过氧化物酶体增殖物激活的受体调节在非酒精性脂肪肝和非酒精性脂肪性肝炎中的治疗潜力

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摘要

A long neglected hepatic manifestation of the metabolic syndrome, non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH) arise as serious health burden with alarming global prevalence. The disease complex is currently attracting considerable interest of drug discovery and many experimental approaches are studied in all stages of clinical development. Peroxisome proliferator-activated receptors (PPARs) have a successful history as pharmaceutical targets in the treatment of several aspects of the metabolic syndrome and, therefore, a putative therapeutic value of PPAR modulators in NAFLD/NASH is obvious. However, so far only the PPARα/δ agonist elafibranor has revealed clear efficacy and reached an advanced stage of development while the far more established PPAR subtypes PPARα and PPARγ have disappointed. Still, clinical trial design and population might have obscured beneficial activities and, in addition, synergistic multi-target approaches as well as selective PPAR modulators could generate safer approaches with higher therapeutic efficacy.
机译:长期以来,代谢综合征,非酒精性脂肪性肝病(NAFLD)和非酒精性脂肪性肝炎(NASH)的长期被忽视的肝病表现已成为严重的健康负担,令人震惊的全球患病率。该疾病复合物目前吸引了相当多的药物发现兴趣,并且在临床开发的所有阶段都研究了许多实验方法。过氧化物酶体增殖物激活受体(PPAR)作为治疗代谢综合征多个方面的药物靶标具有成功的历史,因此,PPAR调节剂在NAFLD / NASH中的公认治疗价值是显而易见的。然而,到目前为止,只有PPARα/δ激动剂弹性纤维显示出明显的功效并达到了发展的晚期,而更成熟的PPAR亚型PPARα和PPARγ却令人失望。尽管如此,临床试验设计和人群可能掩盖了有益的活动,此外,协同的多靶点方法以及选择性的PPAR调节剂可以产生具有更高疗效的更安全方法。

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